EP2788041A1 - Antifungal catheter - Google Patents

Antifungal catheter

Info

Publication number
EP2788041A1
EP2788041A1 EP12809906.6A EP12809906A EP2788041A1 EP 2788041 A1 EP2788041 A1 EP 2788041A1 EP 12809906 A EP12809906 A EP 12809906A EP 2788041 A1 EP2788041 A1 EP 2788041A1
Authority
EP
European Patent Office
Prior art keywords
antimicrobial agent
silicone rubber
antimicrobial
catheter
tube
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP12809906.6A
Other languages
German (de)
English (en)
French (fr)
Inventor
Anthony J. Conway
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rochester Medical Corp
Original Assignee
Rochester Medical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rochester Medical Corp filed Critical Rochester Medical Corp
Publication of EP2788041A1 publication Critical patent/EP2788041A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00—Catheters; Hollow probes
    • A61M25/0017—Catheters; Hollow probes specially adapted for long-term hygiene care, e.g. urethral or indwelling catheters to prevent infections
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
    • A61L29/08—Materials for coatings
    • A61L29/085—Macromolecular materials
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
    • A61L29/04—Macromolecular materials
    • A61L29/06—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
    • A61L29/14—Materials characterised by their function or physical properties, e.g. lubricating compositions
    • A61L29/16—Biologically active materials, e.g. therapeutic substances
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00—Catheters; Hollow probes
    • A61M25/0009—Making of catheters or other medical or surgical tubes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04—Polysiloxanes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
    • A61L2300/404—Biocides, antimicrobial agents, antiseptic agents

Definitions

  • the present invention relates to sustained release antimicrobial cannulas or catheters, which are either implantable or insertable into a human body. These devices have an antimicrobial agent incorporated within the device, which diffuses out in situ to prevent the proliferation or colonization of microbes in regions adjacent to the exterior of the cannula or catheter.
  • the present invention also relates to methods for making the same, products made by these methods, and methods of using the sustained release antimicrobial cannulas or catheters, to prevent proliferation, colonization or continued viability of a microbial population in regions adjacent to the exterior of the respective cannula or catheter.
  • catheters are a cannula or tube like device which is inserted into a portion of a person's body in order to transport fluids or gases in or out of that particular portion of the body. In passing through any particular portion of the body in order to reach its destination, the catheter will come into contact with various tissues in the body. For example, a catheter used to drain ones bladder (such as a "Foley" catheter) must pass through the urethral tract in order to reach the bladder. A nasogastric catheter must pass through the nasal passageway and the esophagus in order to reach the stomach. Some catheters, such as these, are inserted through existing passageways in order to reach their destinations, while others are inserted through surgically created passageways.
  • a catheter used to drain ones bladder such as a "Foley" catheter
  • a nasogastric catheter must pass through the nasal passageway and the esophagus in order to reach the stomach.
  • a sustained release antimicrobial cannula for residence within a portion of a human body through which aqueous biological fluids can pass.
  • the sustained release antimicrobial cannula comprises a tube having an inner surface, defining an internal lumen, and an outer surface.
  • the tube has a polymeric matrix and an antimicrobial agent residing within at least a portion of the polymeric matrix, wherein the polymeric matrix can include cured silicon rubber.
  • the antimicrobial agent can, for example, be a finely divided nitrofuran such as nitrofurazone, a finely divided paraben antifungal (e.g., methyl paraben, ethyl paraben, or propyl paraben), or combinations thereof.
  • a finely divided nitrofuran such as nitrofurazone
  • a finely divided paraben antifungal e.g., methyl paraben, ethyl paraben, or propyl paraben
  • Such antimicrobial agent is soluble in water and is effective to prevent proliferation of certain microbes in an otherwise growth supporting aqueous environment when dissolved in the aqueous environment to the limit of its solubility therein at 37° C.
  • the antimicrobial agent can diffuse out of the polymeric matrix and into an aqueous biological environment when the polymeric matrix comes into contact with such an aqueous biological environment.
  • at least a finite portion of the polymeric matrix proximate the outer surface includes an amount of from about 10 to about 60% by weight of the antimicrobial agent, and the antimicrobial agent in the finite portion of the polymeric matrix and the solubility of the antimicrobial agent cooperate to provide a potential for sustained release diffusion of the antimicrobial agent into the aqueous biological fluids within the human body, during normal therapeutic use of the cannula therein, so long as the aqueous biological fluids are not saturated with the antimicrobial agent, such that the antimicrobial agent within the finite portion of the polymeric matrix can continue to diffuse into the aqueous biological fluids within the human body in an amount effective to prevent proliferation of certain microbes immediately adjacent to the cannula in aqueous biological environments for a period of not less than about three weeks.
  • the cannula is a urinary catheter for residence within a urinary tract, for example a "Foley" catheter having an expandable balloon cavity, a second lumen in communication with the expandable balloon cavity and a coating on at least a portion of the exterior surface of the catheter proximate the balloon cavity which is for example a cured silicon rubber polymeric matrix incorporating an antimicrobial agent capable of diffusing out of the polymeric matrix in aqueous environments.
  • the rate of diffusion of the antimicrobial agent from the polymeric matrix can increase when the expandable balloon portion expands.
  • the present invention provides a sustained release antimicrobial cannula or catheter which can be used on a long-term basis to reduce or eliminate the incidence of urinary tract infections in patients having a chronic need for catheterization.
  • the present invention provides a catheter having a large percentage of active antimicrobial agent incorporated into a cured silicon rubber outer coating.
  • the antimicrobial agent is a finely divided nitrofuran compound such as nitrofurazone having a solubility of about 0.2% by weight or less, a pafaben antifungar(e.g., methyl parab ⁇ nTethyl paraben; or propyl parab ⁇ n)7of combinations thereof.
  • a pafaben antifungar e.g., methyl parab ⁇ nTethyl paraben; or propyl parab ⁇ n7of combinations thereof.
  • the mean particle size of the antimicrobial agent particles is about 200 microns or less in order to create a very smooth outer surface on the cannula or catheter. This is important to reduce the incidence of irritation of the tissues within the urinary tract.
  • the mean particle size of the antimicrobial agent particles is about 100 microns or less enabling the incorporation of this agent at an even higher percentage in the polymeric matrix, while still retaining the desired smoothness, flexibility and durability of the outer coating.
  • Figure 1 is a transverse schematic view of an extruded double lumen tube in partial cross-section
  • Figure 2 is a cross-sectional view of the extruded double lumen tube as seen from the line 2-2 of Figure 1 ;
  • Figure 3 is a transverse schematic view of the tube shown in partial cross- section in Figure 1 after an opening is punched in the outer surface;
  • Figure 4 is a cross-sectional view of the tube as shown from the line 4—4 of Figure 3;
  • Figure 5 is a transverse schematic view of the double lumen tube shown in partial cross-section in Figure. 3 after a portion of the first lumen has been filled with a polymeric bonding composition;
  • Figure 6 is a cross-sectional view of the tube as seen from the line 6—6 of Figure 5;
  • Figure 7 is a transverse schematic view of the double lumen tube shown in partial cross-section in Figure 5 after a tip is affixed to a distal end of the tube;
  • Figure 8 is a schematic view of a portion of a rack used to retain a plurality oj- ⁇ gg citing a series ⁇ of ⁇ ipping steps;
  • Figure 9 is a transverse schematic view of an intermediate tube in partial cross-section similar to the tube shown in Figure 7 at an intermediate stage of manufacture prior to the first of a series of dipping steps;
  • Figure 10 is a transverse schematic view of an intermediate tube in partial cross-section similar to that shown in Figure 9, but following a first dipping step wherein the outer surface is coated with a bond preventing agent up to the point designated by line A;
  • Figure 11 is a cross-sectional view of the intermediate tube of Figure 10 as shown from the line 11—11;
  • Figure 12 is a view of an intermediate tube in partial cross-section similar to that shown in Figure 10, but after a subsequent dipping step or steps in which the coating of bond preventing agent on a portion of the outer surface of the intermediate tube has been removed;
  • Figure 13 is a transverse schematic view of a portion of a balloon catheter formed from the intermediate tube shown in Figure 12 in partial cross-section, following a plurality of dipping steps to create an overcoat layer;
  • Figure 14 is a cross-sectional view of the balloon catheter shown in Figure 13 from the line 14-- 14;
  • Figure 15 is transverse schematic view of a portion of a coated balloon catheter formed from the balloon catheter shown in Figure 13 in partial cross- section, following a further coating step to create an outer antimicrobial release layer;
  • Figure 16 is a cross-sectional view of the balloon catheter shown in Figure 15 from the line 16-- 16;
  • Figure 17 is a transverse schematic view of a Foley catheter made in accordance with the present invention following testing and cleaning and showing sectional views of portions thereof;
  • Figure 18 is a schematic view of a portion of the Foley catheter shown in Figure 15, but with the balloon portion of the catheter shown when expanded;
  • Figure 19 is a schematic illustration of apparatus used to automate the production of balloon catheters in accordance with the present invention.
  • FIGS. 1a, 20b and 20c are flow charts representing certain steps in accordance with the present invention.
  • Figure 21 is a transverse schematic view of an alternate extruded double lumen tube in partial cross-section
  • Figure 22 is a cross-sectional view of the alternate extruded double lumen tube as seen from the line 22—22 of Figure 21 ;
  • Figure 23 is a transverse schematic view of the alternate tube shown in Figure 21 after an opening is punched in the outer surface
  • Figure 24 is a cross-sectional view of the alternate tube as shown from the line 24-24 of Figure 23;
  • Figure 25 is a transverse schematic view of the alternate double lumen tube shown in Figure 23 after a portion of the first lumen has been filled with a polymeric bonding composition;
  • Figure 26 is a cross-sectional view of the alternate tube as seen from the line 26--26 of Figure 25;
  • Figure 27 is a transverse schematic view of the alternate double lumen tube shown in Figure 25 after a tip is affixed to a distal end of the tube;
  • Figure 28 is a schematic view of a portion of a rack or pallet used to retain a plurality of tubes during a series of dipping steps;
  • Figure 29 is a transverse schematic view of an alternate intermediate tube in partial cross-section similar to the alternate tube shown in Figure 27 at an intermediate stage of manufacture following the first of a series of dipping steps which creates a coating of bond preventing lubricating agent on the outer surface;
  • Figure 30 is a transverse schematic view of the alternate intermediate tube shown in Figure 29, but following a second dipping step wherein the coating of bond preventing lubricating agent on the outer surface has been partially removed;
  • Figure 31 is a cross-sectional view of the intermediate tube of Figure 30 as shown from the line 31—31;
  • Figure 32 is a transverse schematic view of the alternate intermediate tube shown in Figure 30, but after a subsequent dipping step creating a second coating of bond preventing lubricating agent on a portion of the outer surface removed form the portion which remains coated by the first coating;
  • ig Ure is aTtransverse schelmtic ⁇ view of li ⁇ e ⁇ termed eWoe shown in Figure 32, but after yet another dipping step or step designed to remove the second coating from a further portion of the outer surface;
  • Figure 34 is a cross-sectional view of the balloon catheter shown in Figure 33 from the line 34-34;
  • Figure 35 is a transverse schematic view of the intermediate tube shown in Figure 33, following a further dipping step or steps to create an overcoat layer;
  • Figure 36 is a transverse schematic view in partial cross-section of a portion of an alternate balloon catheter formed from the alternate intermediate tube shown in Figure 35, following a further dipping step or steps to create an outer antimicrobial release layer;
  • Figure 37 is a perspective view of a portion of the balloon catheter shown in Figure 35 in partial cross-section, but wherein the balloon catheter has been severed through the sleeve cavity and the remaining portion of the sleeve has been twisted to demonstrate its independence of the outer surface of the extruded double lumen tube used to make the balloon catheter;
  • Figure 38 is a transverse schematic view of the balloon catheter shown in Figure 35, but in partial cross-section, but including an end piece and showing a sectional view of a portion of the catheter wherein the balloon portion of the catheter is expanded;
  • Figure 39 is a transverse schematic view in partial cross-section of yet another embodiment of the present invention similar to that shown in Figure 38;
  • Figure 40 is a transverse schematic sectional view showing a portion of the catheter shown in Figure 39 when inserted in a urethral tract;
  • Figure 41 is a schematic illustration of apparatus used to automate the production of catheters in accordance with the present invention.
  • Figure 42a, 42b and 42c are flow charts illustrating certain steps in methods in accordance with the present invention.
  • Figure 43 is a transverse schematic view of another alternate extruded tube in partial cross-section.
  • Figure 44 is a transverse schematic view of an alternate intermediate tube formed from the alternate extruded tube shown in Figure 43;
  • Figure 45 is a schematic view in partial cross-section of a portion of an alternate rack or pallet usedTo ⁇ etSh ⁇ pluraliyof altemaTe ⁇ inlermediatell ⁇ during a series of steps designed to provide the tubes with overcoat layers of a polymeric bonding composition, wherein a single alternate intermediate tube like that shown in Figure 44 is shown secured to a single support rod following a first dipping step wherein a portion of the outer surface of the alternate intermediate tube is coated with a bond preventing lubricating material;
  • Figure 46 is a transverse schematic view of the alternate intermediate tube shown in Figure 43 and 44, but following a second dipping step wherein the coating of bond preventing lubricating material on the outer surface of the alternate intermediate tube has been partially removed;
  • Figure 47 is a transverse sectional schematic view of the alternate
  • Figure 48 is a transverse sectional schematic view of the alternate
  • Figure 49 is a transverse schematic view in partial cross-section of an elongated catheter in accordance with the present invention which is made from the alternate intermediate tube shown in Figure 48.
  • the present invention provides cannulas and/or catheters 4, 5 having an outer antimicrobial release layer 61 which is capable of a sustained release or diffusion of antimicrobial agent into aqueous environments proximate the outer antimicrobial release layer 61.
  • the outer antimicrobial release layer 61 is for example a cured silicon rubber polymeric matrix. Impregnated within the cured silicon rubber polymeric matrix is at least one antimicrobial agent.
  • the antimicrobial agent utilized in the invention can be utilized to inhibit or kill rnicrob ⁇ such ⁇ s bacteria, fungi, and or viruses and for example inhibit or kill at least bacteria and fungi.
  • An antimicrobial agent is a compound, drug or composition containing a compound or drug that inhibits the growth of or kills one or more microbes, such as bacteria, fungi, and/or viruses.
  • the microbes such as bacteria, fungi, and/or viruses.
  • an antimicrobial agent is utilized to inhibit the growth of or kill bacteria and fungi, and are therefore referred to as antibacterial and antifungal agents.
  • an antimicrobial agent is an antibacterial agent, an antifungal agent, or combinations thereof.
  • the antimicrobial agent includes an antibacterial and an antifungal agent.
  • the antibacterial agent and the antifungal agent can be a nitrofuran compound and a paraben antifungal (e.g., methyl paraben, ethyl paraben, or propyl paraben), respectively.
  • the antibacterial agent is nitrofurazone and the antifungal agent is a paraben antifungal (e.g.; methyl paraben, ethyl paraben, or propyl paraben).
  • nitrofuran compounds utilized in the invention have the formula below:
  • R is a carbon continuing moiety such as that disclosed, for example, in K. Miura et al., entitled “The Nitrofurans,” in Progress in Medicinal Chemistry (Vol. 5), pp. 320-381, (G. P. Ellis & G. B. West (eds.), Plenum Press, New York, N.Y. (1967), the disclosure of which is incorporated by reference herein.
  • Suitable nitrofurans are those which are soluble in water and have antimicrobial activity in aqueous environments.
  • Suitable nitrofuran compounds include nitrofurantoin, nitrofurazone, nidroxyzone, nifuradene, furazolidone, furaltidone, nifuroxime, nihydrazone, nitrovin, nifurpirinol, nifurprazine, nifuraldezone, nifuratel, nifuroxazide, urfadyn, nifiirtimox, triafur, nifurtoinol, nifurzide, nifurfoline, nifuroquine, and derivatives of the same, and other like nitrofurans which are both soluble in water and possess antibacterial and antimicrobial activity.
  • References to each of the above cited nitrofuran compounds may be found in the Merck Index, specifically the ninth edition (1976) and the eleventh edition (1989) thereof, published by Merck & Co.,—
  • nitrofuran compounds include nitrofuran compounds which are medically acceptable for topical use, for example topical use for mucosal surfaces.
  • the nitrofuran compounds have a solubility of about 0.2% by weight or less in water at a pH of about 6 and temperature of about 25° C. In an embodiment, the nitrofuran compounds have a solubility in water of about 0.2 to about 0.001% by weight in water at a pH of about 6 and a temperature of about 25° C. In an embodiment, the solubility of the nitrofuran compound under these conditions is about 0.1% by weight or less.
  • an antimicrobial agent which is effective to prevent the proliferation and colonization of microbes within aqueous systems, and that it is also important to have an antimicrobial agent which is not so soluble in aqueous systems that it will immediately diffuse out of the polymeric matrix within which it is incorporated. These characteristics are important in order to provide a sustained release of the antimicrobial agent into the aqueous systems so as to provide for long-term antimicrobial activity. It will also be appreciated that the rapid release or diffusion of the antimicrobial agent into an aqueous environment in contact with the outer antimicrobial release layer 61 will also result in irregularities in the surface of the catheter or cannula 4, 5 which may irritate adjacent tissues within the patient's urinary tract.
  • the outer surface of the outer antimicrobial release layer 61 is smooth so as to minimize the incidence of irritation to the tissues of the urinary tract. In order to provide a smoother outer surface, it is important to minimize the particle size of the finely divided
  • the mean particle diameter of the antimicrobial agent particles is for example about 200 microns or less, about 150 microns or less, or about 100 microns or less.
  • the size of the mean particle diameter can be controlled by filtering the larger particles out of the mixture used to coat the intermediate tubes used to make the finished catheters or cannulas 4, 5.
  • the outer antimicrobial release layeF61 include3 ⁇ 4e ⁇ 3 ⁇ 4n ⁇
  • the silicone fluid allows the cured silicone polymeric matrix to provide for greater diffusion of aqueous media into and out of the polymeric matrix.
  • the silicone fluid is desirable because it provides a softer, more pliable polymeric matrix which is also easier to elongate.
  • the incorporation of the silicone fluid along with the minimization of the mean particle diameter of the antimicrobial agent particles cooperate to maximize the smoothness of the outer surface of the outer antimicrobial release layer 61, and to maximize the structural integrity, softness and stretchability of the release layer 61. The structural integrity is also important so that the amount of the antimicrobial agent incorporated into the release layer 61 can be maximized.
  • antimicrobial agent particles of virtually any size
  • suitable mean particle diameters include less than about 500 microns, about 400 microns or less, about 300 microns or less, or about 200 microns or less, to be able to incorporate more of the agent into the polymeric matrix and still have a soft and pliable polymeric matrix and a smooth outer surface so as to provide commercially acceptable products.
  • the outer antimicrobial release layer 61 for example includes about 2-80% by weight, about 5-70% by weight, about 10-60% by weight, or about 15-55% by weight of the antimicrobial agent in the present invention.
  • the outer antimicrobial release layer 61 may also include an anti- inflammatory agent in amounts similar to the amounts recited herein for the antimicrobial agent.
  • Suitable anti-inflammatory agents are water soluble, antiinflammatory agents such as hydrocortisone, hydrocortisone acetate, hydrocortisone phosphate, hydrocortisone hemisuccinate sodium salt, hydrocortisone tebutate, and the like.
  • any therapeutically acceptable, water soluble anti-inflammatory agent may be used in the present invention in order to reduce inflammation of the tissues adjacent to the present catheter or cannula 4, 5 when inserted in a human body.
  • the hydrocortisone compound has a solubility in water of less than about 0.1% by weight.
  • the present catheter or cannula 4, 5 for example provides an outer antimicrobial release layer 61 having a smoother outer surface such that it minimizes irritation to adjacent tissues.
  • This release layer 61 for example includes about 10-60% by weight of a suitable antimicrobial agent having a mean particle diameter of 200 microns or less.
  • the catheter or cannula 4, 5 of the present invention provides a potential for sustained release of the antimicrobial agent incorporated in the outer antimicrobial release layer 61 for a period of at least about two weeks, for example at least about three weeks, at least about four weeks, or about five weeks.
  • the antimicrobial agent is released for periods of at least about six weeks, seven weeks, eight weeks, or more, depending upon the amount of the solid antimicrobial agent which is incorporated into the release layer 61 and the solubility thereof in water. It will be appreciated, however, that although it is desirable to incorporate a large amount of the antimicrobial agent into the release layer 61, it is also important to retain the elongation characteristics and smoothness which is generally available to cellastic membranes used on similar catheters or cannulas.
  • the rate of release of the antimicrobial agent into the surrounding aqueous environment is dependent on the rate of fluid exchange. It has been observed that 3 milliliters of fluid exchange generally occurs within an average female urinary tract every 24 hours. Because the concentration of the antimicrobial agent in the fluid adjacent to the release layer 61 will generally reach a point of equilibrium with the antimicrobial agent within the release layer 61, the diffusion rate of the antimicrobial agent out of the release layer 61 will be slowed as the concentration reaches maximum solubility for the particular antimicrobial agent incorporated into the release layer 61. As additional fluid passes into the urinary tract and dilutes the fluid already present or washes the fluid out, the diffusion rate will increase.
  • the present invention is designed to attempt to maintain a concentration of the antimicrobial agent in the aqueous fluids within the urethra at a level generally commensurate with the maximum solubility of the antimicrobial agent. It will be appreciated, however, that this will not always be the case.
  • nitrofurazone is the nitrofuran compound of choice and a paraben antifungal (e.g., methyl paraben, ethyl paraben, or propyl paraben) is the antifungal of choice.
  • a paraben antifungal e.g., methyl paraben, ethyl paraben, or propyl paraben
  • a paraben antifungal e.g., methyl paraben, ethyl paraben, or propyl paraben
  • nitrofurazone is desirable, not only because of its limited solubility in water, but also because of its broad antibacterial and
  • Nitrofurazone is also desirable because of its yellow color, which provides an attractive product for commercial presentation.
  • paraben antifungal e.g., methyl paraben, ethyl paraben, or propyl paraben
  • a silicone rubber/nitrofurazone/paraben dispersion or mixture is prepared as follows: 100 grams of nitrofurazone powder and 400 grams paraben is wetted with approximately 10 fluid ounces of 1,1,1 -trichloroethane (Hydrite Chemical Co., LaCrosse, Wis.). This mixture is agitated vigorously.
  • nitrofurazone/paraben/trichloroethane mixture is passed through a filter to remove the larger nitrofurazone and paraben particles.
  • a filter to remove the larger nitrofurazone and paraben particles.
  • two 6-inch cone-shaped filters from TUFCO medium mesh are used back-to-back (one inside the other) to filter the
  • nitrofurazone/paraben/trichloroethane mixture The filtering step is repeated three or four times to remove the larger, oversized particles of nitrofurazone and paraben which will not pass through the medium mesh TUFCO filters.
  • the nitrofurazone/paraben/trichloroethane mixture or dispersion is combined with the silicone rubber dispersion and agitated constantly.
  • the fluid mixture of the solid nitrofurazone and paraben particles in the silicone rubber dispersion is allowed to settle just prior to dipping to form the release layer 61 on the outer surface of the overcoat layer 44 as further discussed herein below. It will be appreciated that the dispersion may be pumped through a single filter or a series of filters designed to provide a nitrofurazone/paraben dispersion having a precise mean particle diameter.
  • the first step in making a balloon catheter in accordance with the present invention is providing a double lumen tube 2, which is for example extruded and made of silicone rubber.
  • the double lumen tube can be made by any known process which yields a double lumen tube.
  • the tube can be made of any resilient polymeric material, for example a biocompatible polymeric material which can be inserted into a human body cavity.
  • the double lumen tube 2 includes a smaller capillary lumen 6 and a larger fluid conduit lumen 8.
  • a capillary lumen access opening 12 is created in an outer surface 14 of the double lumen tube 2.
  • the capillary lumen access opening 12 communicates with the capillary lumen 6.
  • an intermediate tube 3 is subsequently prepared from the double lumen tube 2 shown in Figure 3.
  • a measured amount of a polymeric bonding composition for example uncured silicone rubber or another suitable polymeric bonding material, is injected into the capillary lumen 6 from the distal end 16 of the double lumen tube 2, so that the capillary lumen 6 is filled with a polymeric fill material 18 up to a point just below the capillary lumen access opening 12.
  • a tip 20, for example a rounded silicone rubber tip is then affixed to the distal end 16 of the tube 2 to complete the formation of the intermediate tube 3 shown in Figure 7.
  • the distal end 16 of the tube 2 inserted into a molding apparatus (not shown) designed to mold a tip 20 on the end of the tube 2.
  • an embodiment of the present invention involves securing a plurality of intermediate tubes 3, like the intermediate 3 shown in Figure 7, to a rack or pallet 24.
  • the rack or pallet 24 will include a plurality of support rods 26, each equipped with a retaining clip 28.
  • intermediate tubes 3 are secured on the support rods 26 by engaging individual support rods 26 in the larger of the two lumens, called the fluid conduit lumen 8, and sliding the intermediate tubes 3 up over the support rods 26 until the proximal ends 30 of the intermediate tubes 3 abut against the base of the retaining clips 28 or, for example, the tip 20 of each of the intermediate tubes 3 fits snugly against the distal tip of each of the support rods 26, as shown in Figures 9 and 10.
  • the intermediate tubes 3 can be secured on the support rods 26 without the aid of the retaining clips 28. This is because the extruded double lumen tubes 2 used to make the intermediate tubes 3 generally have a slight bend in one direction or another when they are hung.
  • the pallet 24 can be transferred from place to place, and the intermediate tubes 3 on the pallet 24 can be dipped in a series of baths (see Figure 19) prepared to accomplish a series of process steps.
  • the intermediate tube 3 is made nearly entirely of silicone rubber and is secured upon a support rod 26 made of spring steel.
  • the tip 20 and the fill material 18 of the intermediate tube 3 shown in Figure 7 are made of the same material (silicone rubber) as the double lumen tube 2. Therefore, the tip 20 and the fill material 18 form integral portions of the intermediate tube 3, which is shown in Figures 9-16 as an integral polymeric unit made of a single material.
  • the first step in the automated coating or dipping process of forming the balloon portion 32 of the balloon catheter 4 is to coat the intermediate tubes 3 with a bond preventing agent, for example a removable bond preventing agent.
  • a bond preventing agent for example a removable bond preventing agent.
  • this is accomplished by dipping each of the tubes 3 on the pallet 24 simultaneously into a first dip tank 33 containing a bath 33a of a removable bond preventing agent, for example a material which forms a semi-solid film on surfaces when cooled on contact followed by an opportunity for drying.
  • Such materials include petroleum jelly or petrolatum, other oil base substances which form a semi-solid upon cooling to room temperature, liquid soaps which dry to form a semi-solid, aqueous soap or detergent solutions, aqueous or oil based film forming solids emulsions, and the like.
  • hot petrolatum is used, and in another, a liquid soap is used, for example Liquid Ivory Soap from Proctor & Gamble, Cincinnati, Ohio.
  • the agent adheres to the outer surface 14 of the intermediate tube 3, and enters the capillary lumen access opening 12 and runs up into the capillary lumen 6.
  • the agent is petrolatum, which is heated to about 140°-160° F, for example about 150°F. At these temperatures, the petrolatum will run up into the capillary lumen 6 through the capillary lumen access opening 12 with the assistance of the "capillary effect", which draws the fluid into the capillary lumen 6 to the level of the petrolatum in the first tank 33.
  • the bond preventing agent in the first tank 33 is liquid soap at room temperature (about 62°-74°).
  • the liquid soap forms of semi-solid just as the hot petrolatum did as it cooled.
  • soap is easier to remove from the capillary lumen 6 and the balloon cavity 54.
  • the tubes 3 are then dipped in a series of dip tanks (see Figure 19) provided to remove the bond preventing agent from a portion 14a of the outer surface 14 below the dashed line designated B.
  • the intermediate tubes 3 now partially coated with bond preventing agent between the dashed lines designated A and B as shown in Figure 12, are dipped in a polymeric bonding composition, for example silicone rubber, in a step or steps provided to coat the intermediate tube 3 to create the balloon catheter 4 shown in Figures 13-14.
  • a polymeric bonding composition for example silicone rubber
  • the intermediate tube 3 is dipped in silicone rubber in two or more successive dipping steps so that the resulting overcoat layer includes at least an underlying and an overlying layer, 43 and 44 respectively, which form an integral part of the balloon catheter 4 and are bonded together and to the outer surface 14 in the portions thereof, 14a and 14b, which are located below the dashed line designated B and above the dashed line designated A, respectively.
  • the portion 14b above line A was not coated prior to the final dipping steps designed to provide the overcoat layer 42, and the portion 14a below line B was stripped of its coating prior to those steps.
  • the balloon catheter 4 is then dipped in the silicone rubber in two or more successive dipping steps so that the resulting overcoat layer includes at least an underlying and an overlying layer, 43 and 44 respectively, which form an integral part of the balloon catheter 4 and are bonded together and to the outer surface 14 in the portions thereof, 14a and 14b, which are located below the dashed line designated B and above the dashed line designated A, respectively.
  • the end piece 46 can include a cap 48 for closing a proximal end access opening 49 to the fluid conduit lumen 8 and can be equipped with a luer valve 50 for engagement in and closure of the proximal capillary lumen access upper opening 52
  • the completed balloon catheter 4 Prior to the attachment of the end piece 46 to the balloon catheter 4 to form the completed Foley catheter 5, the completed balloon catheter 4 is for example allowed to air dry to permit solvents in the outer antimicrobial release layer 61 to evaporate and is subsequently cured at an elevated temperature. Care is taken to keep the curing temperature below the boiling temperatures of the solvent so as to prevent unsightly bubbling of the solvent within the overcoat layer 42 or the outer antimicrobial release layer 61. Because the overcoat layer 42 and the outer fungicide release layer 61 are made of the same polymeric bonding composition, even though each respective layer 42, 61 may be created in a plurality of dipping steps, they are represented in Figures 15-18 as single layers 42, 61.
  • the completed Foley catheter 5 also includes a fluid conduit access opening
  • the fluid conduit access opening 56 communicates with the fluid conduit lumen 8.
  • the access opening 56 is punched into the catheter 5 following the curing steps.
  • two access openings 56, one on either side of the catheter 5 (second access opening 56 not shown) are punched into the catheter 5.
  • the access opening 56 is created before the intermediate tube 4 is dipped in the silicone antimicrobial coating mixture
  • an inner surface layer (not shown), incorporating the fungicide agent 15 is created along an inside of the fluid conduit lumen 8.
  • the end piece 46 is made by a process of injection molding.
  • the proximal end 30 of the balloon catheter 4 is inserted into the injection molding apparatus after the overcoat layer 42 and the release layer 61 have been cured.
  • the polymeric bonding composition for example silicone rubber, is then injected into the mold (not shown) and the end piece 46 is molded onto the proximal end 30 of the balloon catheter 4 to make the completed Foley catheter 5 shown in Figure 17.
  • the completed catheter 5 is tested to see if it is functional and if it has any leaks.
  • This testing can be done before or after the fluid conduit access opening 56 is created in the exterior surface 62 to communicate with the fluid conduit lumen 8. Care is taken during such testing to avoid any needless exposure of the release layer 61 or any other antimicrobial impregnated matrices to aqueous environments.
  • the proximal capillary lumen access opening 52 is slipped over a hot water nozzle (not shown), and a measured amount of a hot aqueous solution, for example water or water containing a trace of surfactant, at a temperature of between about 120°- 160° F, for example about 140° F, is pumped into the capillary lumen 6 from a standard hot water heater (not shown) by a commercially available water pump (not shown) such that the balloon portion 58 is expanded.
  • a hot aqueous solution for example water or water containing a trace of surfactant
  • the balloon portion 58 of the overcoat layer 42 is the portion of the overcoat layer 42 which is not bonded to the outer surface 14 of the intermediate tube 3.
  • the balloon portion 58 of the overcoat layer 42 cooperates with the portion 14c of the outer surface 14 which remained coated with the bond preventing agent prior to the step of dipping the intermediate tube 3 in the polymeric bonding composition, to define a balloon cavity 54.
  • the balloon cavity 54 communicates with the capillary lumen 6 via the capillary lumen access opening 12. When the hot water solution is pumped or injected into the capillary access lumen 6 to test the completed catheter 5 and the balloon portion 58, the balloon portion 58 and the balloon cavity 54 are expanded.
  • the water solution will also remove the remaining bond preventing agent in the balloon lumen 54 and the capillary lumen 6 when it is removed. Although some of the bond preventing agent may come out of the capillary lumen 6 via the proximal capillary lumen access opening 52 during the step of curing the overcoat layer 42, the hot aqueous solution is generally believed to remove most of the bond preventing agent, although a residue may remain.
  • a further test is used to obtain further assurance that there are no leaks in the balloon portion 58.
  • This further test is accomplished by engaging the proximal capillary lumen accessing opening 52 to the nozzle of a commercially available leak tester (not shown).
  • a leak tester (not shown).
  • One such device is a Model No. 6510 Caps Tester from Caps Himmelstein (Hoffman Estates, 111.
  • an electrical switch such as a hand switch or, for example, a foot pedal, is used to release a measured blast of air into the capillary lumen 6.
  • the air When the air is introduced into the capillary lumen 6 it also enters the balloon cavity 54 via the capillary lumen access opening 12 and inflates the balloon portion 58 and, thereby, expands the balloon cavity 54.
  • the leak tester is designed to sense any loss of pressure once the balloon portion 58 is inflated, and will given an indication, therefore, if there are any measurable leaks.
  • the completed catheters 5 that have passed all tests are then packaged, for example in a material which breathes such as TyvekTM (from DuPont), and boxed. The boxes are then sterilized with ETO (ethylene oxide) and then stored for shipment.
  • ETO ethylene oxide
  • balloon fabrication is almost completely automated. Entire sets of balloon catheters 4 are manufactured simultaneously.
  • pallet 24 has 400 spring steel support rods 26 attached to a pallet in 20 rows of 20 rods, wherein each of the rods 26 is about 1 inch from each adjacent rod.
  • Double lumen tubing (not shown) is for example made by an extrusion process which is known to those of skill in the art. The tubes 2 are cut to length as the tubing leaves the extruder (not shown).
  • An opening 12 is created in the outer surface 14, for example with a hollow drill bit or tube (not shown), so as to communicate with the capillary lumen 6.
  • a rounded tip 20 is for example formed at the distal end 16 of the double lumen tube 2 by inserting the tube 2 in a molding device (not shown).
  • 400 of the intermediate tubes 3 are then mounted vertically on rigid spring steel support rods 26 on a pallet 24 in the manner previously described.
  • the pallet 24 is then moved via a transporting mechanism 22 (see Figure 19) over a series of dip tanks as follows in one of these embodiments:
  • the tank is raised so as to immerse the intermediate tubes 3 into the petrolatum to such a depth that the petrolatum reaches the proximal end of the desired balloon location.
  • the dip tank 33 is then lowered and a portion of the outer surface 14 of the intermediate tubes 3 are coated with petrolatum. This portion extends from the point at which the proximal end of the balloon portion 58 will begin to the distal end of the tip 20 of the intermediate tube 3.
  • the pallet 24 is then automatically advanced and stopped over a second dip tank 35 which contains white USP petrolatum heated to about 120° C. (about 250° F).
  • the second dip tank 35 is raised so as to immerse the intermediate tubes 3 into the super-heated petrolatum so that the super-heated petrolatum comes into contact with the petrolatum coating on outer surface 14 of the intermediate tube 3 from the prior dipping step up to a location where a distal end of the balloon portion 58 will end.
  • the second dip tank 35 is then lowered.
  • This dipping step causes the coating of petrolatum from the prior dipping step to be largely removed from a portion 14a of the outer surface 14 of the intermediate tube 3 from a location where the distal end of the balloon lumen 54 will be located (designated by dashed line B) to the distal end 20a of the tip 20 of the intermediate tube 3.
  • Some residual petrolatum may remain on the outer surface 14 of the intermediate tube 3 in this portion 14a of the outer surface 14. However, most of the petrolatum is removed.
  • the pallet 24 is then automatically advanced and stopped over a third dip tank 37 containing mineral spirits heated to about 200° F.
  • the third dip tank 37 is then raised so as to immerse the intermediate tubes 3 into the mineral spirits to the same depth as they were immersed in the super-heated petrolatum in the second dip tank 35.
  • the tank 37 is then lowered and all but a trace amount of the petrolatum is removed from the portion 14a of the outer surface 14 below the portion 14c of the outer surface 14, which will eventually be proximate the balloon lumen 54.
  • the fourth tank 39 is then raised to immerse the intermediate catheters 3 to the same depth as previously immersed in the second and third tanks 35 and 37, thereby removing essentially all traces of the petrolatum from this portion 14a of the outer surface 14.
  • the intermediate catheter tube 3 now has a band 38 of semi-solid petrolatum located around the axial circumference of the intermediate tube 3 in the location where the balloon cavity 54 will be created.
  • the petrolatum not only coats the portion 14c of the outer surface 14 located in this area, but also fills a portion of the capillary lumen 6 and plugs the capillary lumen access opening 12, which will eventually be used to inflate the balloon portion 58 of the completed Foley catheter 5.
  • overcoat layer 42 and the balloon portion 58 of the overcoat layer 42 have a desired balloon thickness.
  • the thickness over the overcoat layer 42 and the balloon portion 58 can be, for example, 17.5 thousandths of an inch (plus or minus 2.5 thousandths of an inch).
  • the tank 41 is then lowered, and the overcoat layer 42 is allowed to dry and the solvent is allowed to evaporate for about 15 minutes, for example about 30 minutes or about an hour.
  • the pallet 24 is advanced to a sixth dip tank 43 containing a silicone rubber/nitrofuran compound mixture or dispersion 17, and the tubes 3 are completely immersed again.
  • the tank 43 is lowered.
  • the pallet is then advanced through a drying area where solvents are allowed to evaporate, and then through a heat cure step, where the balloon catheters 4 formed by this process are cured at a temperature just below the boiling point of any solvent used in any of the silicone rubber dip solutions for an hour or two. For toluene this temperature is about 200°
  • the balloon catheters 4 are allowed to cool and are then removed from the support rods 26.
  • the proximal ends 30 of each of the balloon catheters 4 is then inserted into an injection molding apparatus (not shown), which forms the end piece 46 of the completed Foley catheter 5.
  • balloon catheters are produced as follows:
  • the pallet 24 is stopped over a first tank 33, which contains a liquid soap (Liquid Ivory Soap from Proctor & Gamble Co., Cincinnati, Ohio 45202).
  • the soap is held at room temperature (between about 60°-80° F, for example 65°-72° F).
  • the dip tank 33 is raised so as to immerse the intermediate tubes 3 into the liquid soap so that the soap coats the tubes 3 up to the dashed line designated by the letter A in Figure 10.
  • the dip tank 33 is then lowered and the liquid soap forms a semi-solid coating 38 on the outer surface 14 of each of the intermediate tubes extending from line A to the distal end of the tip 20 of the intermediate tubes 3.
  • the pallet 24 is then automatically advanced and stopped over a second dip tank 35 which contains an aqueous solution containing a trace of a suitable wetting agent or surfactant.
  • a suitable wetting agent or surfactant In an embodiment, three gallons of water is mixed with two ounces of a ' suitable surfactant. The surfactant will generally be less than one percent of the total volume of the solution.
  • the second dip tank 35 is then raised so as to immerse the intermediate tubes 3 in the aqueous fluid up to the dashed line designated by the letter B in Figures 10 and 12.
  • the second dip tank 35 is then lowered and the semi-solid liquid soap coating the portion 14a of the outer surface 14 below the dashed line designated B is substantially removed.
  • the pallet 24 is then automatically advanced and stopped over a third dip tank 37 containing water.
  • the third dip tank 37 is then raised and the intermediate tubes are immersed in the water up to the line designated B as in the prior dipping step.
  • the third dip tank 37 is then lowered and virtually all of the liquid soap is removed from the portion 14a of the outer surface 14 below the line designated B.
  • the pallet 24 is then automatically advanced and stopped over a fourth dip tank 39 containing a low-solids hexamethyl disiloxane silicone rubber solution which is effective to minimize any disruption of the integrity of the liquid soap coating 38 remaining on each of the intermediate tubes proximate the portion 14c of the outer surface 14 where the balloon lumen will be created during subsequent dipping steps (the portion between the dashed lines designated A and B).
  • the fourth tank 39 is then raised to immerse essentially the entire length of each of the intermediate tubes 3 in the silicone rubber solution. It will be appreciated that other organic solvents such as toluene, and the like may be substituted for the hexamethyl disiloxane solvent used in this example.
  • the dipping step can be repeated at subsequent intervals, for example long enough to permit significant solvent evaporation (prior to any subsequent dipping), to add to the thickness of the overcoat layer 42 and the balloon portion 58 of the overcoat layer 42. Further steps, involving different solutions, can also follow.
  • the pallet 24 is then automatically advanced again to a sixth dip tank 43 containing the silicone rubber/antimicrobial compounds fluid mixture described hereinabove.
  • the tubes can be dipped a second time after allowing about 10-15 minutes for drying.
  • the sixth dip tank 43 is then lowered and the silicone rubber/antimicrobial compounds coating the tubes 3 is allowed to dry for about 15 minutes.
  • the automated system that Applicants claim will permit completed Foley catheters 5 to be manufactured at the rate of about 1,600 catheters per hour. Because no handwork is involved, the catheters 5 produced will be consistent and of very high quality.
  • the exterior surface 62 is smoother than hand-glued balloons, and the outside diameter of the balloon portion 58 is essentially identical to the outside diameter of other portions of the completed Foley catheters 5.
  • the applicants' new process will permit direct production cost for silicone rubber balloon catheters of all types to be reduced by about 25-50% over the cost estimated for the prior art silicone rubber balloon catheters.
  • the first step in making an alternate balloon catheter 4' in accordance with the present invention is providing a double lumen tube 2', which is for example extruded and made of silicone rubber.
  • the double lumen tube 2' can be made by any known process which yields a double lumen tube 2'.
  • the tube 2' can be made of any resilient polymeric material, for example a biocompatible polymeric material which can be inserted into a human body cavity.
  • the double lumen tube 2' includes a smaller capillary lumen 6' and a larger fluid conduit lumen 8'.
  • a capillary lumen access opening 12' is created in an outer surface 14' of the double lumen tube 2'.
  • the capillary lumen access opening 12' communicates with the capillary lumen 6'.
  • an intermediate tube 3' is subsequently prepared from the double lumen tube 2' shown in Figure 9.
  • a measured amount of a polymeric bonding composition for example silicone rubber or another suitable polymeric bonding material, is injected into the capillary lumen 6' from the distal end 16' of the double lumen tube 2', so that the capillary lumen 6' is filled with a polymeric fill material 18' up to a point just below the capillary lumen access opening 12'.
  • a tip 20' for example a rounded silicone rubber tip, is then affixed to the distal end 16' of the tube 2' to complete the formation of the intermediate tube 3' shown in Figure 13.
  • the distal end 16' of the tube 2' is inserted into a molding apparatus (not shown) designed to mold a tip 20' on the end of the tube 2'.
  • a process of the present invention involves securing a plurality of intermediate tubes 3', like the intermediate tube 3' shown in Figure 13, to a rack or pallet 24'.
  • the rack or pallet 24' will include a plurality of support rods 26', each equipped with a retaining clip 28'.
  • the intermediate tubes 3' are secured on the support rods 26' by engaging individual support rods 26' in the larger of the two lumens 8', called the fluid conduit lumen 8', and sliding the intermediate tubes 3' up over the support rods 26' until the proximal ends 30' of the intermediate tubes 3' abut against the base of the retaining clips 28' or, for example, the tip 20' of each of the intermediate tubes 3' fits snugly against the distal tip 26a' of each of the support rods 26', as shown in Figures 29 and 30.
  • the intermediate tubes 3' can be secured on the support rods 26' without the aid of the retaining clips 28'.
  • the extruded double lumen tubes 2' used to make the intermediate tubes 3' generally have a slight bend in one direction or another when they are hung. This results in a slight bend in the intermediate tubes 3' that permits the intermediate tube 3' to be secured on a support rod 26' without the aid of a clip 28'.
  • the polymeric materials generally used to make the intermediate tubes 3' they also have a tendency to cling to other surfaces and to offer resistance to movement of a surface along a surface of this material as do most polymeric tubes including those tubes 2 described hereinabove.
  • the pallet 24' can be transferred from place to place, and the intermediate tubes 3' on the pallet 24' can be dipped in a series of baths prepared to accomplish a series of process steps.
  • the intermediate tube 3' is made entirely of silicone rubber and is secured upon a support rod 26' made of spring steel.
  • the tip 20' and the fill material 18' of the intermediate tube 3' shown in Figure 27 are made of the same material (silicone rubber) as the double lumen tube 2'. Therefore, the tip 20' and the fill material 18' for example form integral portions of the intermediate tube 3', which is shown in Figures 29-36.
  • the first step in the automated coating or dipping process of forming the resilient sleeve 44' and the balloon portion 32' of the balloon catheter 4' is to coat the intermediate tubes 3' with a bond preventing lubricating agent or substance 38', for example a removable bond preventing lubricating agent.
  • a bond preventing lubricating agent or substance 38' for example a removable bond preventing lubricating agent.
  • this is accomplished by dipping each of the tubes 3' on the pallet 24', simultaneously into a first dip tank 33' containing a bath 33a' of a removable bond, for example a material which forms a semi-solid film on surfaces when cooled on contact followed by an opportunity for drying.
  • Such materials include petroleum jelly or petrolatum, other oil base substances which form a semi-solid upon cooling to room temperature, liquid soaps which dry to form a semi-solid, aqueous soap or detergent solutions, aqueous or oil based film forming solids emulsions, and the like.
  • hot petrolatum is used, and in another, a liquid soap is used, for example Liquid Ivory Soap from Proctor & Gamble, Cincinnati, Ohio.
  • the agent or substance 38' adheres to the outer surface 14' of the intermediate tube 3', and occupy the capillary lumen access opening 12' and the capillary lumen 6'.
  • the agent is petrolatum, which is heated to about 140°- 160° F, for example about 150° F. At these temperatures, the petrolatum will run up into the capillary lumen 6' through the capillary lumen access opening 12' with the assistance of the "capillary effect", which draws the fluid into the capillary lumen 6' to the level of the petrolatum in the first tank 33'.
  • the bond preventing agent in the first tank 33' is liquid soap at room temperature (about 62°-74° F).
  • intermediate tubes 3' are coated when they are dipped in a first bath 33 a' which contains petrolatum which is maintained at a temperature effective to permit the petrolatum to coat the outer surface 14' of the tube while limiting the degree to which the petrolatum runs into the smaller lumen 6'.
  • the petrolatum will run into the first lumen access opening 12', but, for example, will not run very far into the smaller lumen 6'.
  • the temperature of the petrolatum in the first tank 33' is for example maintained at about 40°-80, about 50°-70°, about 55°-65°, or about 60° C for this purpose.
  • the intermediate tube 3' is coated with the bond preventing lubricating agent 38' up to a location on the surface 14' of the intermediate tube 3' proximate the dashed line A shown in Figure 29 by dipping the intermediate tube 3' into the first dip tank 33' up to that point.
  • the outer surface 14' of the intermediate tube 3' is stripped of the bond preventing lubricating agent 38' up to a location proximate the dashed line designated B in Figures 29 and 30.
  • This can be accomplished by one or more dipping steps in accordance with the methods for stripping particular lubricating agents as described herein below.
  • the intermediate tube is then for example coated as shown in Figure 30 between the locations proximate the dashed lines A and B.
  • the intermediate tube 3' shown in Figure 30 is then dipped in a subsequent dip tank holding a second bond preventing agent.
  • the liquid soap can be employed, although petrolatum and other agents will also work.
  • the intermediate tube 3' shown in Figure 30 is dipped into the tank up to a point on the outer surface 14' of the intermediate tube 3' proximate the dashed line C so as to coat the portion of the intermediate tube 3' from the lowest portion of the tip 20' up to the location proximate the dashed line designated C.
  • any of the bond preventing lubricating agents enumerated above may be used.
  • the bond preventing lubricating agent is hot petrolatum heated to about 130°-150° F, for example about 140° F (about 60° C), or liquid soap at room temperature (about 62°-74° F).
  • petrolatum will cool and solidify to form a semi-solid coat 39' on the outer surface 14' and a semi- solid filling 34' in the capillary lumen 6' and the capillary lumen access opening 12' which cooperate to plug the capillary lumen access opening 12' as shown in Figure 32.
  • the intermediate tube is then subjected to a further dipping step wherein the intermediate tube shown in Figure 32 is dipped in one or more dip tanks so as to strip the coating of bond preventing agent 39' from the portion of the intermediate tube 3' below a location on the outer surface 14' proximate the dashed line designated D in Figures 32 and 33 so as to strip the tube of bond preventing agent below that location.
  • the tubes 3' are then dipped in a series of dip tanks (see Figure 41) provided to coat the intermediate tube 3' with a polymeric bonding composition, for example silicone rubber, in a step or steps provided to form the overcoat layer 42', and, following a short drying interval, an outer fungicide release layer 6 ⁇ is created by dipping the intermediate tube 3' into the silicone rubber/nitrofurazone/paraben compound mixture or dispersion 17 in the last dip tank 57'.
  • the outer release layer 6 ⁇ is then air dried for about an hour, and then cured.
  • the release layer 61 ' is coated only over the uncured silicone rubber overcoat layer 42'.
  • the catheter 4' is cured in a hot liquid bath at 160° F for about 15 min., and then cured in hot air at 200° F for an additional hour. This prevents the sleeve from drooping when the contents of the sleeve are raised to high temperatures.
  • the intermediate tube 3' is dipped in silicone rubber in two or more successive dipping steps so that the resulting overcoat layer 42' includes underlying and an overlying layers (not shown), which form an integral part of the balloon catheter 5' and are bonded together, and to the outer surface 14' in the portions thereof, 14a', 14b' and 14d', which are located below the dashed line designated D, between the dashed lines designated B and C, and above the dashed line designated A, respectively.
  • the portion 14d' above line A was not coated prior to the final dipping steps designed to provide the overcoat layer 42', and the portion 14a' below line D was stripped of its coating prior to those steps.
  • the proximal end 30' of the balloon catheter 5' is secured to an end piece 46' to form a completed Foley catheter 4' (shown in Figure 38).
  • the end piece 46' can include a cap 48' for closing a proximal end access opening 49' to the fluid conduit lumen 8' and can be equipped with a luer valve 50' for engagement in and closure of the proximal capillary lumen access upper opening 52'
  • the sleeved balloon catheter 5' Prior to the attachment of the end piece 46' to the sleeved balloon catheter 5' to form the completed sleeved Foley catheter 4', the sleeved balloon catheter 5' is for example allowed to air dry to permit solvents in the overcoat layer 42' to evaporate and is subsequently cured at an elevated temperature. Care is taken to keep the curing temperature below the boiling temperatures of the solvent so as to prevent unsightly bubbling of the solvent within the overcoat layer 42'. Because the overcoat layer 42' is for example made of the same polymeric bonding composition, even though it may be created in a plurality of dipping steps, it is represented in Figures 35-39 as a single overcoat layer 42'.
  • the completed Foley catheter 4' also includes a fluid conduit access opening 56' in an exterior surface 62' of the completed Foley catheter 4'.
  • the fluid conduit access opening 56' communicates with the fluid conduit lumen 8'.
  • the resilient sleeve 44' which includes both the overcoat layer 42' and the release layer 6 , not only has a narrower thickness than the inner wall 21 ' of the catheter 5', but it is also more flexible, more stretchable, and for example less rigid than the inner wall 2 .
  • the lubricating substance 38' contained in the sleeve cavity 45' permits the sleeve 44' to slide along and in respect to the outer surface 14' while in lubricated contact therewith and when stretched independently thereof.
  • the resilient sleeve 44' can be twisted in respect to the inner wall 21 ' without twisting the inner wall 21 ' or the respective lumens, 6' and 8'.
  • the resilient sleeve 44' can also be stretched without stretching the inner wall 2 ⁇ of the catheter 5'. As stated hereinabove, this enables the resilient sleeve 44' to stay in relative contact with or in adherence to adjacent body tissues (not shown) with which the resilient sleeve 44' is in contact with even when the remaining portions of the sleeved balloon catheter 5', such as the inner wall 21', are forced to move in response to forces impacting on the catheter 5' at other points along its length.
  • the resilient sleeve 44 can also change from its initial circumferential shape to a more ribbon-like oval shape in order to match the shape or contour of the passageway in which it resides.
  • the volume of the sleeve cavity 45' will for example increase the outside diameter of the catheter proximate the sleeve portion at least about 5%, for example about 10%, about 20%, about 25%, about 35%, or about 50%. It is conceivable that applications will also be found where the thickness of the lubricating substance in the sleeve cavity 45 is increased so as to increase the volume of the sleeve cavity such that the outside diameter of the catheter proximate the sleeve 44 will be increased from about 50 to 100, or 50 to 200% or more depending on the particular application.
  • the sleeve be soft and compliant so that it can conform to the shape of the particular passageway in which it resides and, at the same time fill the passageway so as to limit the passage of fluids along either the wall of the passageway or the exterior surface of the catheter, and at the same time, to allow the inner conduit portion of the catheter move relatively independently of the exterior surface of the sleeve 44' of the catheter.
  • the end piece 46' is made by a process of injection molding.
  • the proximal end 30' of the sleeved balloon catheter 5' is inserted into an injection molding apparatus (not shown) after the overcoat layer 42' and the release layer 6 ⁇ have been cured.
  • the end piece 46' can be added to the
  • a polymeric bonding composition for example silicone rubber, is then injected into the mold (not shown) and the end piece 46' is molded onto the proximal end 30' of the balloon catheter 5' to make the completed Foley catheter 4' shown in Figure 38.
  • the completed catheter 4' is tested to see if it is functional and if it has any leaks. This testing can be done before or after the fluid conduit access opening 56' is created in the exterior surface 62' to communicate with the fluid conduit lumen 8'.
  • the proximal capillary lumen access opening 52' is slipped over a hot water nozzle (not shown), and a measured amount of a hot aqueous solution, for example water or water containing a trace of surfactant, at a temperature of between about 120°- 160° F, for example about 140° F, is pumped into the capillary lumen 6' from a standard hot water heater (not shown) by a commercially available water pump (not shown) such that the balloon portion 58' is expanded.
  • a hot aqueous solution for example water or water containing a trace of surfactant
  • the balloon portion 58' of the overcoat layer 42' is the portion of the overcoat layer 42' which is not bonded to the outer surface 14' of the intermediate tube 3' proximate a balloon cavity 54'.
  • the balloon portion 58' of the overcoat layer 42' cooperates with the portion 14c' of the outer surface 14' which remained coated with the bond preventing agent prior to the step of dipping the intermediate tube 3' in the polymeric bonding composition, to define the balloon cavity 54'.
  • the balloon cavity 54' communicates with the capillary lumen 6' via the Capillary lumen access opening 12'.
  • the hot water solution When the hot water solution is pumped or injected into the capillary access lumen 6' to test the completed catheter 4' and the balloon portion 58', the balloon portion 58' and the balloon cavity 54' are expanded. If there is a significant lack of integrity in the balloon portion 58' it will be exposed when the water is introduced in this manner. In addition to testing the balloon portion 58', the water solution will also remove the remaining bond preventing agent in the balloon lumen 54' and the capillary lumen 6' when it is removed.
  • the hot aqueous solution is generally believed to remove most of the bond preventing agent, although a residue may remain.
  • a further test is used to obtain further assurance that there are no leaks in the balloon portion 58.
  • This further test is accomplished by engaging the proximal capillary lumen accessing opening 52' to the nozzle of a commercially available leak tester (not shown).
  • a leak tester (not shown).
  • One such device is a Model No. 6510 Caps Tester from Caps Himmelstein (Hoffman Estates, 111.
  • an electrical switch such as a hand switch or, for example, a foot pedal, is used to release a measured blast of air into the capillary lumen 6'.
  • the air When the air is introduced into the capillary lumen 6' it also enters the balloon cavity 54' via the capillary lumen access opening 12' and inflates the balloon portion 58' and, thereby, expands the balloon cavity 54'.
  • the leak tester is designed to sense any loss of pressure once the balloon portion 58' is inflated, and will given an indication, therefore, if there are any measurable leaks.
  • the completed sleeved Foley catheters 4' that have passed all tests are then packaged, for example in a material which breathes such as Tyvek (from DuPont), and boxed.
  • the boxes are then sterilized with ETO (Ethylene Oxide) and then stored for shipment.
  • ETO Ethylene Oxide
  • the present invention provides an elongated catheter 4'" (see Figure 49) having an interior surface 7"' and an exterior surface 9"'.
  • the interior surface 7"' defines a lumen 8'".
  • the elongated catheter 4"' is for example made from a tube 2"' (see Figure 43) which is eventually coated with an overcoat layer 42"' of a resilient polymeric material which binds to an outer surface 14"' of the tube 2"' unless the bonding of the polymeric material is prevented by other materials or means on the outer surface 14"'.
  • the overcoat layer 42 of the elongated catheter 4"' in accordance with the present invention includes a sleeve 44"' which encircles a sleeve cavity 45"' which contains lubricating material 38"'.
  • the lubricating material or substance 38'" is effective to permit the sleeve 44"' to slide along the outer surface 14"' of the tube 2"' proximate the sleeve 44"' while in lubricated contact with the outer surface 14"'.
  • the lubricating material serves to separate the soft outer sleeve 44"' from the tube 2'", such that the outer sleeve 44"' provides a soft, cushioned, compliant exterior surface which can adapt and conform under slight pressures to the shape of the passageway in which it is inserted or residing.
  • the amount of the lubricating substance 38"' and the sleeve cavity 45"' can be minimized to provide for only a limited increase in the outer diameter of the catheter proximate the outer sleeve 44'".
  • the outer sleeve 44"' is coated with an outer fungicide release layer 6 ⁇ " similar to that described hereinabove.
  • a soft, cushioned, compliant sleeve which can adapt its shape is desirable.
  • the elongated catheter 4'" is for example made of a flexible elastomeric material such as latex, silicone rubber or the like, most for example silicone rubber.
  • the lubricating material or substance 38"' is for example any biocompatible lubricating substance which is effective to permit respective polymeric surfaces to slide with respect to one another when in lubricated contact therewith.
  • the lubricating substance 38"' is a hydrophobic oil or other petroleum based product or a water-soluble soap, detergent or the like, either of which is effective to lubricate polymeric surfaces and to generally prevent bonding thereto by other polymeric substances when coated thereby.
  • the lubricating substance 38"' is petrolatum.
  • the first step in making an elongated catheter 4"' in accordance with the method of the present invention is to provide a tube 2"' having an outer surface 14"' and an inner surface 7"' defining a first lumen 8"'.
  • the distal end 16"' of the tube 2"' is for example inserted into a molding apparatus (not shown) designed to mould a tip 20"' on the distal end 16"' of the tube 2"' to form the intermediate tube 3"' (see Figure 44).
  • the intermediate tube 3"' is then secured on a support rod 26"' of a rack or pellet 2 4"' which for example includes a plurality of support rods 26"'.
  • a plurality of intermediate tubes 3"' are secured on the plurality of support rods prior to subjecting the intermediate tubes 3"' secured on the support rods 26"' to a series of dipping steps.
  • the outer surface is coated from the lowest portion of the tip 20"' up to a location on the outer surface 14"' designated by the dashed line A, as shown in Figure 45, with the lubricating substance. Subsequently, the lubricating substance coating the outer surface 14 of the tube below a location proximate the dashed line designated B, as shown in Figures 45 and 46, is stripped from the outer surface 14"' and the tip 20"'.
  • the intermediate tube 3'" is then coated with a resilient polymeric bonding composition which forms the overcoat layer 42"'.
  • the overcoat layer 42"' bonds to the tip 20"' and a portion of the outer surface 14a'" below the dash line designated B, and to a portion of the outer surface 14b'" above the line designated A.
  • the overcoat layer 42"' forms a sleeve 44"' which encircles the lubricating material 38"' coating the portion of the outer surface 14a'" between the dash lines designated A and B, which cooperates with the sleeve 44"' to define the sleeve cavity 45"' in which the lubricating material 38"' proximate the sleeve 44"' is contained.
  • an outer fungicide release layer 6 " is formed and a pair of fluid conduit openings 56 are for example created, for example punched, to permit fluid to pass into or out of the lumen 8"' proximate the distal end 16"'.
  • the overcoat layer 42"' and the wall 1 ⁇ " of the tube 2"' are shown in Figure 49 to be separate elements, when made of identical polymeric materials, the wall 11 "' and the overcoat layer 42"' will be bonded together where they interface with one another so that it is virtually impossible to distinguish between the two and so that there is for example no part line in spite of the fact that a part line is shown in Figures 47 and 49. In certain embodiments, where these elements are enjoined together, it will be appreciated that they form an integral membrane or wall.
  • balloon and sleeve fabrication is almost completely automated. Entire sets of sleeved balloon catheters 5' are manufactured simultaneously.
  • the pallet 24 has 400 spring steel support rods 26 attached to a pallet in 20 rows of 20 rods, wherein each of the rods 26 is about 1 inch from each adjacent rod.
  • Single and double lumen tubing (not shown) is for example made by extrusion processes known to those of skill in the art.
  • the tubes 2 and 2' are cut to length as the tubing leaves the extruder (not shown).
  • An opening 12' is created in the outer surface 14' of the double lumen tubes 2', for example with a hollow drill bit or drill tube (not shown), so as to communicate with the capillary lumen 6' in those tubes 2'.
  • the distal portion 6a' of the capillary lumen 6' located between the distal end 16' of the tube 2' and the capillary lumen access opening 12', is then injected with a measured amount of a polymeric bonding composition, for example silicone rubber, so that the distal portion 6a' is filled and sealed.
  • a rounded tip 20' is then formed at the distal end 16' of the double lumen tube 2', for example by inserting the tube 2' in a molding device (not shown).
  • FIG 39 another embodiment of the present invention is illustrated in this embodiment of the present invention as sleeved Foley catheter 4". It is very similar to the catheter shown in Figure 38 except that the space between the balloon cavity 54" and the sleeve cavity 45" has been decreased so that it will accommodate the urethral sphincter of the bladder.
  • the volume of the lubricating substance 38"" in the sleeve cavity 45" is significantly more than that shown in Figure 38. This is accomplished by increasing the thickness of the lubricating substance 38 which is coated onto the intermediate tube carrying the manufacturing process.
  • the increase in the thickness of the lubricating substance 38" allows the sleeved Foley catheter 4" to provide a very soft, “cushy”, conforming exterior surface 9" proximate the sleeve 44" which can accommodate variations in the surfaces with which the catheter 4" comes into contact.
  • the sleeved Foley catheter 4" shown in Figure 39 is shown when inserted into a urethral tract 74 of a woman 70 the balloon portion 58" of the catheter 4" resides within the bladder 72 of the woman 70. The balloon portion 58" is expanded to retain the catheter 4" in the urethral tract 74.
  • the harsh volume of lubricating substance 38" in the sleeve cavity 45" is shown to provide a exterior surface 9" proximate the sleeve 44" which conforms to the wall of the urethral tract 74.
  • the lubricating substance 38" also allows the inner wall 46" or conduit portion 46" of the catheter 4" to move back and forth within the urethral tract 74" to a limited degree without disrupting the interface between the exterior surface 9" proximate the sleeve 44" and the adjacent body tissues of the urethral tract. This allows the catheter 4" to move in all directions to a limited degree without disrupting this interface, thereby increasing the comfort of the patient in which the catheter 4" resides.
  • 400 of the intermediate tubes 3' are then mounted vertically on rigid spring steel support rods 26' on a pallet 24' in the manner previously described.
  • the pallet 24' is then moved via a transporting mechanism 22 (see Figure 28) over a series of dip tanks as follows in the following.
  • the pallet 24' is stopped over a first tank 33', which contains white USP petrolatum heated to about 60° C (about 140° F).
  • the tank is raised so as to immerse the intermediate tubes 3' into the petrolatum to such a depth that the petrolatum reaches the proximal end of the desired sleeve location.
  • the dip tank 33' is then lowered and a portion of the outer surface 14' of the intermediate tubes 3' are coated with petrolatum. This portion extends from the general point at which the proximal end of the resilient sleeve 44' will begin, to the distal end 20a' of the tip 20' of the intermediate tube 3'.
  • This step is repeated when it is desirable to build up the thickness of the lubricating substance and the resulting volume of the sleeve cavity so as to increase the resulting increase in the outside diameter of the particular catheter over the circumferential diameter of the conduit portion or tube 2 or 2' of this present invention.
  • the pallet 24' is then automatically advanced and stopped over a second dip tank 35' which contains white USP petrolatum heated to about 120° C (about 250° F).
  • the second dip tank 35' is raised so as to immerse the intermediate tubes 3' into the super-heated petrolatum so that the super-heated petrolatum comes into contact with the petrolatum coating 38' on outer surface 14' of the intermediate tube 3' from the prior dipping step up to a general location where a distal end of the resilient sleeve 44' will end.
  • the second dip tank 35' is then lowered.
  • This dipping step causes the coating of petrolatum from the prior dipping step to be largely removed from the portions 14a' the outer surface 14' below a location where the distal end of the resilient sleeve 44' will be generally located (designated by dashed line B) to the distal end 20a' of the tip 20' of the intermediate tube 3'.
  • Some residual petrolatum may remain on the outer surface 14' of the intermediate tube 3' in this area of the outer surface 14'. However, most of the petrolatum is removed.
  • the pallet 24' is then automatically advanced and stopped over a third dip tank 37' containing mineral spirits heated to about 200° F.
  • the third dip tank 37' is then raised so as to immerse the intermediate tubes 3' into the mineral spirits to the same depth as they were immersed in the super-heated petrolatum in the second dip tank 35'.
  • the tank 37' is then lowered and all but a trace amount of the petrolatum is removed from the outer surface 14' located generally below the dashed line B, which will eventually be proximate the sleeve 44'.
  • the fourth tank 40' is then raised to immerse the intermediate catheters 3 to the same depth as previously immersed in the second and third tanks 35' and 37+, thereby removing essentially all traces of the petrolatum from this portion of the outer surface 14'.
  • the intermediate catheter tube 3' now has a band 38' of semi-solid petrolatum located around the axial circumference of the intermediate tube 3' in the location where the sleeve cavity 45' will be created.
  • the pallet 24' is then stopped over a fifth, sixth, seventh and eighth dip tank, 4 ⁇ , 43', 5 ⁇ and 53', respectively, where the steps enumerated in steps A, B, C, and D, respectively, are repeated with the following variation.
  • the intermediate tubes 3' are immersed only up to a location proximate the dashed line designated C as shown in Figures 18 and 19.
  • the intermediate tubes 3' on the pallet 24' are only immersed up to a location proximate the dashed line D as shown in Figures 32 and 33.
  • the petrolatum is stripped from the portion 14a' of the outer surface 14' located below the location proximate the dashed line designated line D.
  • the petrolatum not only coats the portion 14c' of the outer surface 14' located in this area, but also fills a portion of the capillary lumen 6' and plugs the capillary lumen access opening 12', which will eventually be used to inflate the balloon portion 58' of the completed Foley catheter 4'.
  • This step can be subsequently repeated at intervals, for example allowing time for significant solvent evaporation, either in the same tank or in a subsequent tank containing a greater concentration of silicone rubber, until the overcoat layer 42' and the balloon portion 58' of the overcoat layer 42' have a desired balloon thickness.
  • the dip tank 55' is then lowered, and the overcoat layer 42' is allowed to air dry for about 15 minutes.
  • the pallet 24' is advanced to a tenth dip tank 57 containing a silicone
  • the thickness of the resilient sleeve 44' and the balloon portion 58' can be 17.5 thousandths of an inch (plus or minus 2.5
  • the concentration of silicone rubber in the subsequent tanks are for example greater than the concentration of the silicone rubber in the ninth tank 51. It is also desirable to alter the silicone rubber used in a final coating to provide greater sheen and a smoother finish, however, the concentration and the solvent may be adjusted as deemed appropriate.
  • the pallet 24' is then advanced through a drying area where solvents are allowed to evaporate, and then through a two port (liquid/hot air) heat cure step, where the sleeved balloon catheters 5' formed by this process are cured, first in a hot liquid bath at 160° F for 15 minutes, and then in hot air (200° F), or at a temperature just below the boiling point of any solvent used in any of the silicone rubber dip dispersions, for an hour. For toluene this temperature is about 200° F.
  • the sleeved balloon catheters 5' are allowed to cool and are then removed from the support rods 26'.
  • the proximal ends 30' of each of the balloon catheters 4 is then inserted into an injection molding apparatus (not shown), which forms the end piece 46' of the completed sleeved Foley catheter 4'.
  • the completed Foley catheters 5 are then finished by punching a fluid conduit access opening 56' in the exterior surface 6 ⁇ such that it communicates with the fluid conduit lumen 8' in a location below or distal to the balloon portion 58' of the overcoat layer 42'.
  • methods of the present invention include the following steps:
  • balloon catheters are produced as follows:
  • this step can be repeated to increase the thickness of the lubricant coating 38', as well as the ultimate volume of the sleeve cavity 45' and the size of the outside diameter of the catheter 5' proximate the sleeve 44'.
  • the pallet 24' is then stopped over a fifth dip tank 4 ⁇ , which contains a liquid soap (Liquid Ivory Soap from Proctor & Gamble Co., Cincinnati, Ohio 45202).
  • the soap is held at room temperature (between about 6°-80° F, for example 65°-72° F).
  • the fifth dip tank 4 ⁇ is raised so as to immerse the intermediate tubes 3' into the liquid soap so that the soap coats the tubes 3' up to the dashed line designated by the letter C in Figure 32.
  • the dip tank 4 ⁇ is then lowered and the liquid soap forms a semi-solid coating 40' on the outer surface 14' of each of the intermediate tubes 3' extending from line designated C to the distal end 20a' of the tip 20' of each of the intermediate tubes 3'.
  • the pallet 24 is then automatically advanced and stopped over a sixth dip tank 43' which contains an aqueous solution containing a trace of a suitable wetting agent or surfactant.
  • a suitable wetting agent or surfactant In an embodiment, three gallons of water is mixed with two ounces of a suitable surfactant. The surfactant will generally be less than one percent of the total volume of the solution.
  • a sixth dip tank 43' is then raised so as to immerse the intermediate tubes 3' in the aqueous fluid up to the dashed line designated by the letter D in Figures 32 and 33.
  • the sixth dip tank 43' is then lowered and the semi-solid liquid soap coating the portion 14a' of the outer surface 14' below the dashed line designated D is substantially removed.
  • the pallet 24' is then automatically advanced and stopped over a eighth dip tank 53' containing a low-solids silicone rubber/solvent dispersion which is effective to minimize any disruption of the integrity of the liquid soap coating 40' remaining on each of the intermediate tubes proximate the portion 14c' of the outer surface 14' where the balloon cavity 54 will be created during subsequent dipping steps (the portion between the dashed lines designated C and D).
  • the eighth tank 53' is then raised to immerse intermediate tubes 3' in the silicone rubber dispersion.
  • any suitable solvent for providing a suitable dispersion of silicone rubber and coating the particular lubricating agent may be used. It is also believed to be possible to use aqueous solvents.
  • this step can be repeated at subsequent intervals, for example long enough to permit significant solvent evaporation, to add to the thickness of the overcoat layer 42' and the balloon portion 58' of the overcoat layer 42'.
  • further steps, involving different solutions can also follow.
  • the fourth dip tank 39' is then lowered and the silicone rubber, coating portions of the outer surface 14' as well as the coating of petrolatum 38' and the coating of soap 40', is allowed to dry.
  • the pallet 24' is then advanced again to a ninth dip tank 55' containing a different silicone rubber dispersions having a solids content which is higher than the solids content in the eighth dip tank 53'.
  • the intermediate tubes 31 ' are immersed again in the subsequent silicone rubber dispersion when the ninth dip tank 55' is raised.
  • the ninth dip tank 55' is then lowered, and the silicone rubber, coating the tubes 3', is allowed to dry.
  • the pallet 24' is then automatically advanced again to a tenth dip tank 53 containing a silicone rubber/nitrofuran/paraben compound fluid mixture 17' including a silicone rubber and silicone fluid in trichloroethane, mixed with a nitrofuran compound, for example with furazone and a paraben antifungal, for example paraben particles having a mean particle diameter of 100 microns or less.
  • a silicone rubber/nitrofuran/paraben compound fluid mixture 17' including a silicone rubber and silicone fluid in trichloroethane, mixed with a nitrofuran compound, for example with furazone and a paraben antifungal, for example paraben particles having a mean particle diameter of 100 microns or less.
  • the automated system that Applicants claim will permit completed sleeved Foley catheters 4' to be manufactured at the rate of about 1,600 catheters per hour. Because virtually no handwork is involved in the balloon and sleeve construction, the catheters 4' produced will be consistent and of very high quality.
  • the exterior surface 62' is smoother than hand-glued balloons, and the outside diameter of the balloon portion 58' is essentially identical to the outside diameter of other portions of the completed Foley catheters 4'. It will be appreciated that larger outside diameter balloon portions are undesirable since they are somewhat more difficult to insert and withdraw, and cause additional trauma upon withdrawal.
  • the applicants' new process will permit direct production cost for silicone rubber balloon catheters of all types to be reduced by about 25-50% over the cost estimated for the prior art silicone rubber balloon catheters.
  • the term “configured” describes a system, apparatus, or other structure that is constructed or configured to perform a particular task or adopt a particular configuration.
  • the term “configured” can be used interchangeably with other similar phrases such as arranged and configured, constructed and arranged, adapted and configured, adapted, constructed, manufactured and arranged, and the like.
EP12809906.6A 2011-12-08 2012-12-06 Antifungal catheter Withdrawn EP2788041A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161568290P 2011-12-08 2011-12-08
US13/705,695 US20130150828A1 (en) 2011-12-08 2012-12-05 Antifungal catheter
PCT/US2012/068249 WO2013086195A1 (en) 2011-12-08 2012-12-06 Antifungal catheter

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EP2788041A1 true EP2788041A1 (en) 2014-10-15

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KR (1) KR20140100973A (pt)
CN (1) CN104053460A (pt)
BR (1) BR112014010305A2 (pt)
IN (1) IN2014DN03170A (pt)
MX (1) MX2014005144A (pt)
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WO (1) WO2013086195A1 (pt)

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US20130150828A1 (en) 2013-06-13
KR20140100973A (ko) 2014-08-18
BR112014010305A2 (pt) 2017-04-18
IN2014DN03170A (pt) 2015-05-22
WO2013086195A1 (en) 2013-06-13
RU2014122868A (ru) 2016-02-10
CN104053460A (zh) 2014-09-17

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